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Published on: September 3, 2021
Inhibition of angiogenesis in liver metastases by carboxyamidotriazole (CAI)
K J Luzzi1, H J Varghese, I C MacDonald
1Department of Medical Biophysics, University of Western Ontario, London, Canada.
Abstract:
Carboxyamidotriazole (CAI), an inhibitor of calcium-mediated signal transduction, is a promising new cytostatic anti-cancer drug which has entered Phase II clinical trials, and for which multiple modes of action have been proposed. We tested the hypothesis that CAI can inhibit tumor angiogenesis in vivo. The ability of orally administered CAI to inhibit experimental metastases of B16F1 melanoma cells in mouse liver was assessed. A computer-assisted stereological technique was then used to analyze images from histological sections of CAI-treated vs. control livers; the vascular volume percentage (percentage of tumor volume consisting of functional microvessels) was determined to assess the effect of CAI on tumor angiogenesis. CAI treatment significantly reduced the size (8 x reduction in volume; P = 0.02) but not the number of metastases. In association with this reduction in tumor size, CAI significantly decreased the vascular volume percentage within metastases by at least a factor of two (P = 0.001). A reduction in both number of microvessels/mm2 and microvessel size (cross-sectional area) was found to contribute to this decrease. CAI treatment did not affect the vascular volume percentage of normal liver tissue surrounding metastases (P = 0.8). This study documents for the first time that CAI can inhibit tumor angiogenesis within metastases in vivo.
Insights
Carboxyamidotriazole (CAI), an anti-cancer drug, significantly reduced melanoma metastasis size in mice by inhibiting tumor angiogenesis. This novel finding highlights CAI
Area of Science:
- Oncology
- Pharmacology
- Cancer Biology
Background:
- Carboxyamidotriazole (CAI) is a novel cytostatic anti-cancer drug inhibiting calcium-mediated signal transduction.
- CAI is currently in Phase II clinical trials with proposed multiple modes of action.
- Tumor angiogenesis is a critical process for tumor growth and metastasis.
Purpose of the Study:
- To investigate the potential of CAI to inhibit tumor angiogenesis in vivo.
- To assess the effect of CAI on experimental liver metastases of B16F1 melanoma cells in mice.
Main Methods:
- Oral administration of CAI to mice with experimental liver metastases.
- Computer-assisted stereological analysis of histological sections to determine vascular volume percentage.
- Quantification of microvessel number and size within metastases.
Main Results:
- CAI treatment significantly reduced melanoma metastasis size by 8-fold (P = 0.02).
- CAI significantly decreased vascular volume percentage within metastases by over 50% (P = 0.001).
- This decrease in vascularization was due to reduced microvessel number and size, without affecting normal liver vasculature.
Conclusions:
- CAI effectively inhibits tumor angiogenesis within metastases in vivo.
- CAI demonstrates a significant anti-angiogenic effect on melanoma liver metastases.
- This study provides the first evidence of CAI's anti-angiogenic activity in vivo.
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